Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. * Perform feasibility, site identification, selection and evaluation, supporting initial list of sites and recruitment targets * Manages sites and site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. * Collaborates with Regional and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.)
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